AccessGUDID - DEVICE: GIALLOY CB (ESRL58901011)

GUDID

Device Identifier (DI) Information

Brand Name: GIALLOY CB
Version or Model: 5890101 bedruckt SRL 12 x 1 kg
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: SRL Dental GmbH

Primary DI Number: ESRL58901011
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 313446764 *Terms of Use

Device Description: Aufbrennfähige Nichtedelmetall-Dental-Gusslegierung auf Kobalt-Basis, Typ 4 / NPM Cobalt-based dental alloy for casting, type 4 Bedruckt SRL 12 x 1 kg

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
35857	Dental casting non-noble alloy	A material composed primarily of non-noble metals [e.g., includes alloys such as cobalt-chrome (Co-Cr), nickel-chromium, titanium (Ti)] intended for use in the fabrication of a dental cast [i.e., a positive copy of a part of the oral anatomy made in an impression (mould), such as a dental crown] or dental restorations and appliances (e.g., porcelain-fused-to-metal crowns and bridge restorations). It is typically available in the form of small ingots or bars that are melted and poured into an impression. After application, this device cannot be reused.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EJH	Alloy, Metal, Base

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 92edabe9-053c-4425-b668-823db102a671
Public Version Date: December 10, 2018
Public Version Number: 1
DI Record Publish Date: November 08, 2018